Evidence map›Paper›PMID 31933648›Full record

ArticleStem cells international2019

Paracrine Proangiogenic Function of Human Bone Marrow-Derived Mesenchymal Stem Cells Is Not Affected by Chronic Kidney Disease.

Femke C C van Rhijn-Brouwer, Bas W M van Balkom, Diana A Papazova, Diënty H M Hazenbrink, Anke J Meijer, Isaac Brete, Vidalmar Briceno, Arjan D van Zuilen, Raechel J Toorop, Joost O Fledderus and 2 more

Abstract read
In one paragraph

Article in Stem cells international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Article
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  4. Article
  5. Extracellular Vesicles in Transplantation.Frontiers in immunology · 2022
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  7. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Femke C C van Rhijn-BrouwerDepartment of Nephrology and Hypertension, Regenerative Medicine Center Utrecht, UMC Utrecht, Utrecht University, Uppsalalaan 8, 3584 CT, Utrecht, Netherlands.ORCID https://orcid.org/0000-0002-7777-646X
Bas W M van BalkomDepartment of Nephrology and Hypertension, Regenerative Medicine Center Utrecht, UMC Utrecht, Utrecht University, Uppsalalaan 8, 3584 CT, Utrecht, Netherlands.
Diana A PapazovaDepartment of Nephrology and Hypertension, Regenerative Medicine Center Utrecht, UMC Utrecht, Utrecht University, Uppsalalaan 8, 3584 CT, Utrecht, Netherlands.
Diënty H M HazenbrinkDepartment of Nephrology and Hypertension, Regenerative Medicine Center Utrecht, UMC Utrecht, Utrecht University, Uppsalalaan 8, 3584 CT, Utrecht, Netherlands.
Anke J MeijerDepartment of Nephrology and Hypertension, Regenerative Medicine Center Utrecht, UMC Utrecht, Utrecht University, Uppsalalaan 8, 3584 CT, Utrecht, Netherlands.
Isaac BreteDepartment of Nephrology and Hypertension, Regenerative Medicine Center Utrecht, UMC Utrecht, Utrecht University, Uppsalalaan 8, 3584 CT, Utrecht, Netherlands.
Vidalmar BricenoDepartment of Nephrology and Hypertension, Regenerative Medicine Center Utrecht, UMC Utrecht, Utrecht University, Uppsalalaan 8, 3584 CT, Utrecht, Netherlands.
Arjan D van ZuilenDepartment of Nephrology and Hypertension, Regenerative Medicine Center Utrecht, UMC Utrecht, Utrecht University, Uppsalalaan 8, 3584 CT, Utrecht, Netherlands.
Raechel J TooropDepartment of Vascular Surgery, UMC Utrecht, Utrecht University, Heidelberglaan 100, 3584 CX, Utrecht, Netherlands.
Joost O FledderusDepartment of Nephrology and Hypertension, Regenerative Medicine Center Utrecht, UMC Utrecht, Utrecht University, Uppsalalaan 8, 3584 CT, Utrecht, Netherlands.
Hendrik GremmelsDepartment of Nephrology and Hypertension, Regenerative Medicine Center Utrecht, UMC Utrecht, Utrecht University, Uppsalalaan 8, 3584 CT, Utrecht, Netherlands.ORCID https://orcid.org/0000-0002-7818-620X
Marianne C VerhaarDepartment of Nephrology and Hypertension, Regenerative Medicine Center Utrecht, UMC Utrecht, Utrecht University, Uppsalalaan 8, 3584 CT, Utrecht, Netherlands.ORCID https://orcid.org/0000-0002-3276-6428

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCell-based therapies are being developed to meet the need for curative therapy in chronic kidney disease (CKD). Bone marrow- (BM-) derived mesenchymal stromal cells (MSCs) enhance tissue repair and induce neoangiogenesis through paracrine action of secreted proteins and extracellular vesicles (EVs). Administration of allogeneic BM MSCs is less desirable in a patient population likely to require a kidney transplant, but potency of autologous MSCs should be confirmed, given previous indications that CKD-induced dysfunction is present. While the immunomodulatory capacity of CKD BM MSCs has been established, it is unknown whether CKD affects wound healing and angiogenic potential of MSC-derived CM and EVs.

methodsMSCs were cultured from BM obtained from kidney transplant recipients (

resultsHealthy and CKD BM MSCs exhibited similar differentiation capacity, proliferation, and senescence-associated

conclusionsOur results indicate that MSCs have an intrinsic capacity to produce proangiogenic paracrine factors, including EVs, which is not affected by donor health status regarding CKD. This suggests that autologous MSC-based therapy is a viable option in CKD.

Identifiers

PMID31933648
PMCPMC6942892

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.